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01 1M/s Ami Lifesciences
02 1M/s Sriam Labs Pvt Ltd
03 1M/s. Elder Pharmaceuticals Ltd.
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01 1Flavoxate Hydrochloride (BP/EP)
02 1Flavoxate Hydrochloride (BP/Ph. Eur)
03 1Flavoxate Hydrochloride BP/USP
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01 1WC-0054
02 1WC-0228
03 1WC-249
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01 3India
Flavoxate Hydrochloride BP/USP
Date of Issue : 2022-08-11
Valid Till : 2025-06-26
Written Confirmation Number : WC-0054
Address of the Firm : Block No. 82/B, ECP Road, At & Post. Karakhadi, Tal-Padra, City Karakhadi -39145...
Flavoxate Hydrochloride (BP/EP)
Date of Issue : 2013-08-30
Valid Till : 2016-07-02
Written Confirmation Number : WC-249
Address of the Firm : A-36, MIDC Industrial Area, Patalganga, Village-Kaire. Tal-Khalapur, Dist. Raiga...
Flavoxate Hydrochloride (BP/Ph. Eur)
Date of Issue : 2019-08-13
Valid Till : 2022-08-12
Written Confirmation Number : WC-0228
Address of the Firm : Sy No.505 Padmati Somaram Road Bibinagar Village and Mandal Nalgonda Dist AP
33
PharmaCompass offers a list of Flavoxate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Flavoxate manufacturer or Flavoxate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flavoxate manufacturer or Flavoxate supplier.
PharmaCompass also assists you with knowing the Flavoxate API Price utilized in the formulation of products. Flavoxate API Price is not always fixed or binding as the Flavoxate Price is obtained through a variety of data sources. The Flavoxate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Urispas manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urispas, including repackagers and relabelers. The FDA regulates Urispas manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urispas API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Urispas manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Urispas supplier is an individual or a company that provides Urispas active pharmaceutical ingredient (API) or Urispas finished formulations upon request. The Urispas suppliers may include Urispas API manufacturers, exporters, distributors and traders.
click here to find a list of Urispas suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Urispas written confirmation (Urispas WC) is an official document issued by a regulatory agency to a Urispas manufacturer, verifying that the manufacturing facility of a Urispas active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Urispas APIs or Urispas finished pharmaceutical products to another nation, regulatory agencies frequently require a Urispas WC (written confirmation) as part of the regulatory process.
click here to find a list of Urispas suppliers with Written Confirmation (WC) on PharmaCompass.
We have 3 companies offering Urispas
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